Literature DB >> 5496557

Enzymatic abnormality of the carrier state in metachromatic leukodystrophy.

N Taniguchi, I Nanba.   

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Year:  1970        PMID： 5496557     DOI： 10.1016/0009-8981(70)90005-7

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN： 0009-8981            Impact factor:   3.786


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  3 in total

1.  Heterozygote detection in MLD. allelic mutations at the ARA locus.

Authors:  D F Farrell
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

2.  Late infantile metachromatic leucodystrophy (MLD). Clinical and diagnostic evaluation in a typical case.

Authors:  L N Rossi; F Vassella; A Bischoff; U N Wiesmann; N Herschkowitz
Journal:  J Neurol       Date:  1975-10-24       Impact factor: 4.849

3.  [Metachromatic leucodystrophy. A genetic study of a familial adult form of metachromatic leucodystrophy (author's transl)].

Authors:  E Czmok; F Regli; K Harzer; H U Benz
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1974
  3 in total

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